An outbreak in an intensive care unit of a strain of methicillin-resistant Staphylococcus aureus sequence type 239 associated with an increased rate of vascular access device-related bacteremia

被引:75
作者
Edgeworth, Jonathan D. [1 ]
Yadegarfar, Ghasem
Pathak, Smriti
Batra, Rahul
Cockfield, Joshua D.
Wyncoll, Duncan
Beale, Richard
Lindsay, Jodi A.
机构
[1] St Thomas Hosp, Dept Infect, London SE1 7EH, England
[2] Kings Coll London, Sch Med, Guys Kings Coll,Dept Infect, Guys & St Thomas Natl Hlth Serv Fdn Trust, London, England
[3] Kings Coll London, Sch Med, Guys Kings Coll,Intens Care Unit, Guys & St Thomas Natl Hlth Serv Fdn Trust, London, England
[4] Kings Coll London, Sch Med, Guys Kings Coll, Dept Nephrol & Transplantat, London, England
[5] St Georges Univ London, Guys Hosp, London, England
[6] St Georges Univ London, Ctr Infect, Dept Cellular & Mol Med, London, England
[7] Univ Southampton, Sch Med, Publ Hlth Sci & Med Stat Grp, Southampton SO9 5NH, Hants, England
关键词
D O I
10.1086/511034
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Patients in intensive care units are at high risk of developing methicillin-resistant Staphylococcus aureus (MRSA) bacteremia. We report an epidemiological and bacterial genomic analysis of a 2-year outbreak in an intensive care unit of a variant of MRSA sequence type 239 ( hereafter designated TW). Methods. A cohort study was conducted to compare risk factors for MRSA bacteremia in patients who acquired TW versus patients who acquired non-TW strains of MRSA. Genetic analysis of TW was performed using multilocus sequence typing and microarray analysis. Results. Patients who acquired TW were more likely than patients who acquired non-TW strains of MRSA to have MRSA isolated from blood samples (47% vs. 13%;) and to have MRSA-positive vascular access P <.001 device-sample cultures (59% vs. 26%;), but less likely to have MRSA isolated from screening swab samples P <.001 ( 30% vs. 71%;). This increased rate of TW bacteremia was confined to the first week after acquisition of P <.001 TW infection. Using Cox regression analysis, the adjusted hazard ratio for bacteremia with TW was 4.5 times that of non-TW strains of MRSA (95% confidence interval, 2.25-9.00; P <.001). Microarray analysis revealed that TW P <.001 had accumulated all detectable mobile genetic elements that were variably expressed by other epidemic strains of MRSA sequence type 239 in the United Kingdom. Conclusions. To our knowledge, this is the first report to provide direct evidence that strains of MRSA can differ in their ability to cause bacteremia. Further genetic and in vitro analysis of the TW strain may provide insight into the mechanism of vascular access device-related bacteremia in the intensive care unit environment.
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页码:493 / 501
页数:9
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